Canonical Allele Identifier: CA2396143318
Gene: ARVCF HGNC NCBI

Linked Data

dbSNP Id: rs1944275074

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19996907G>A , CM000684.2:g.19996907G>A GRCh38
NC_000022.10:g.19984430G>A , CM000684.1:g.19984430G>A GRCh37
NC_000022.9:g.18364430G>A NCBI36
NG_023326.1:g.24880C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263207.8:c.-18-6095C>T MANE Select ENSP00000263207.3:n.-18-6095C>T
ENST00000263207.7:c.-18-6095C>T ENSP00000263207.3:n.-18-6095C>T
ENST00000467828.1:n.158-14816C>T
NM_001670.2:c.-18-6095C>T NP_001661.1:n.-18-6095C>T
XM_005261242.1:c.-18-6095C>T XP_005261299.1:n.-18-6095C>T
XM_005261243.3:c.-18-6095C>T XP_005261300.1:n.-18-6095C>T
XM_005261244.3:c.-18-6095C>T XP_005261301.1:n.-18-6095C>T
XM_006724243.1:c.-18-6095C>T XP_006724306.1:n.-18-6095C>T
XM_006724245.2:c.-18-6095C>T XP_006724308.1:n.-18-6095C>T
XM_006724249.2:c.-18-6095C>T XP_006724312.1:n.-18-6095C>T
XM_006724250.2:c.-18-6095C>T XP_006724313.1:n.-18-6095C>T
XM_011530179.1:c.-18-6095C>T XP_011528481.1:n.-18-6095C>T
XM_011530180.1:c.-18-6095C>T XP_011528482.1:n.-18-6095C>T
XM_011530181.1:c.-18-6095C>T XP_011528483.1:n.-18-6095C>T
XR_937863.1:n.269-6095C>T
XR_937864.1:n.269-6095C>T
XM_005261242.3:c.-18-6095C>T XP_005261299.1:n.-18-6095C>T
XM_005261243.4:c.-18-6095C>T XP_005261300.1:n.-18-6095C>T
XM_005261244.4:c.-18-6095C>T XP_005261301.1:n.-18-6095C>T
XM_006724243.3:c.-18-6095C>T XP_006724306.1:n.-18-6095C>T
XM_006724245.3:c.-18-6095C>T XP_006724308.1:n.-18-6095C>T
XM_006724249.3:c.-18-6095C>T XP_006724312.1:n.-18-6095C>T
XM_006724250.3:c.-18-6095C>T XP_006724313.1:n.-18-6095C>T
XM_011530179.3:c.-18-6095C>T XP_011528481.1:n.-18-6095C>T
XR_937863.2:n.269-6095C>T
NM_001670.3:c.-18-6095C>T MANE Select NP_001661.1:n.-18-6095C>T